US2844541A - Production of dispersions - Google Patents
Production of dispersions Download PDFInfo
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- US2844541A US2844541A US533328A US53332855A US2844541A US 2844541 A US2844541 A US 2844541A US 533328 A US533328 A US 533328A US 53332855 A US53332855 A US 53332855A US 2844541 A US2844541 A US 2844541A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0086—Preparation of sols by physical processes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0004—Preparation of sols
- B01J13/0026—Preparation of sols containing a liquid organic phase
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/924—Significant dispersive or manipulative operation or step in making or stabilizing colloid system
- Y10S516/928—Mixing combined with non-mixing operation or step, successively or simultaneously, e.g. heating, cooling, ph change, ageing, milling
Definitions
- the present linvention relates to la novel method for producing dispersions of variousdi-spersoids in dispers-ing ple.dispersions can be formed ofsodium, sulfur, paran wax and asphalt in various liquid dispersion media such as hydrocarbons, water and the like.
- TheV method is applicable-to the production of l n emulsions offone liquid in another, and of suspensions Vof a solid material in a liquid or semi liquid.
- v c means such as, for example, shaking or agitating a mechanicalst-irrer, but-in general, the method has been .limited to those..materials.which are liquid, or which can easily be brought into a liquid condition.
- My improved method for producing a dispersionof'a lfirst ⁇ substance in a'liquid dispersion medium comprises simultaneously passing the first substance and the liquid together in astream through a heating zone, which may comprise along'tubular pipe arranged within a furnace.lv
- the mixture is heated sufficiently to vap-orize part or all of the liquid dispersion medium to form vapor while maintaining the lirst substance unvaporized.
- the temperature shouldbesutlicientto melt the rst substance if it isv asolidV or semi'solid.v
- themixture and vapor are subjected to highvelocity and turbulent flow to break.
- the eilluent of mixture and vapor is then cooled to condense .the vapor and solidify yany melted particles, thereby forming a dispersion of extremely ne particles of the tirst substance in the liquid dispersion medium.
- Oooling may be accomplished-by circulating a cooling 2 iluid in indirect heat exchange relationshipwith the efuent, or by injecting cool liquid, such as ladditional dispers-ion medium, directly into the effluent for dilution and cooling thereof.
- the method described is operable over a wide range of 4 proportions of dispersion medium and dispersoid.
- the amount of dispersoid can range from as little as 5% of the mixture by weight to as ymuch as 65%.
- the heat-ing zone may be within a pipe having dimensions based upon the desired capacity of aplant. Di-
- ameters may range from '1/2 to 2 inches for example, and lengths may be as little as and as much more or less.
- the invention is generally applicable to the treatmentV and suspensions of various mercury compounds or copper compounds'in oil, sulfur and sodium in oil, sulfur in, p
- the dispersion maybe etiected in the presenceof aj v protective material.
- aj tective material is meant'any dispersingagent, wetting f agentor protective colloid.
- specic examples of such compositions may be mentioned glyptalmresins, 4,gum
- tragacanth alkali metal salts of the higher fattyacids, .i galliacids and their derivatives, agar-agar, glue, ⁇ methyl ,y
- cellulose *sulte cellulose lyes, sodiuml cellulose phthalate, calcium saccharate, sodium cellulose glycollate, gela-Y tin, derivatives of cholesterine, phosphatides, gelloses, v natural and artificial waxes, such as wool waxes, alkylol amine salts, quaternary ammonium compounds, clay, sulfonated tallow, sulfonated oils, alkyl sulfuric esters, kand alkali metal caseinates.
- natural and artificial waxes such as wool waxes, alkylol amine salts, quaternary ammonium compounds, clay, sulfonated tallow, sulfonated oils, alkyl sulfuric esters, kand alkali metal caseinates.
- the materials -to 'be dispersed and the dispersing me-A dium may be introduced into the heating zone in any suitable manner, and the proportions of the different com- In carrying out the ponents may be varied as desired.
- the materials to be dispersed and the dispersing medium are brought together in the desired proportion either by roughly mixing ⁇ the material-s in a single container, or by llowing the materialslfrom separate containersv into amixing tube or chamber.
- the dispersionsystemrproduced may vary Widely in character*dependinglargely lupon ⁇ the materials employed.
- the dispersion medium may contain more than one component, as for example,.solutions of glycerine and Water (preferably 15.-'20.% water) are very desirable dispersion media for sulfur.
- Figs. l and 2 are schematic ⁇ flow diagrams showingl two alternative arrangements of apparatus for carrying out the invention.
- the invention will be Vexemplified l as applied to the production of a dispersion of solid particles of sodium-metal 'in a flowable dispersion medium which is inert to sodium and has'a boiling pointabove 2,844,541 l Patented July 22, 17958 ,il
- themelting point ofsodium including among others the following:
- a mass of sodium metal is melted in the tank 11 by circulating a ⁇ hot hydrocarbon liquid in indirect heat exchange relationship therewith.
- Molten sodium is passed by a pump 13 to the interior of a ⁇ heater 15 and into a long pipe coil 17.
- a liquid dispersion medium such as kerosene from a tank 19 ispassed by a pump21 into conjunction with the stream of molten sodium at the entrance to the coil 17.
- the kerosene should be above the melting point of sodium, 208.1 F., to prevent solidiication. This can be assured by passing the kerosene through a pipe located within the heater 15 before it meets the sodium.
- heating is accomplished by heat exchange with a hot liquid such as a high boiling eutectic mixture of diphenyl and diphenyl oxide sold under the trademark Dowtherm by the Dow Chemical Company (boiling point 258 C.), but heating also may be done by a gas or oil flame.
- a hot liquid such as a high boiling eutectic mixture of diphenyl and diphenyl oxide sold under the trademark Dowtherm by the Dow Chemical Company (boiling point 258 C.)
- heating also may be done by a gas or oil flame.
- the mixture is heated to a temperature high enough to vaporize all or a substantial portion of the kerosene while maintaining the sodium in a molten state.- Consequently, the velocity and turbulence inthe coil increase considerably as liquid vaporizes, the velocity being at least 25 feet per second, preferably above 100 feet per second, and often several thousand feet per second.
- the liquid sodium is converted to tiny molten droplets which impinge against one another and against. the Walls of the tube until they are reduced to an extremely ne particle size such as 10 microns or less and predominantly less than microns, a substantial proportion even being ner than one micron.
- the mixture of liquid and vapor then leaves the pipe coil 17 and enters a cooler 23 wherein the Vapor is ⁇ condensed, the sodium particles are solidified, and a dispersion is formed of extremely ne solid particles of sodium suspended in kerosene. Cooling may be accomplished by ash cooling as the result of the reduced pressure, by circulating cool hydrocarbon liquid indirectly, or by injecting it directly into the effluent Ifrom the pipe coil 17.
- chamber 23 can be a classifier such as a cyclone sep arator to collect the liquid phase while removing vapors therefrom.
- the resulting product can be used for performing various chemical reactions in a well known way, asfor rening hydrocarbons, preparing alcohol-free alkoxides, or for halide condensation reactions.
- a modied system wherein the substance to be dispersed and the dispersing medium are mixed together in a mixer 29 and then passed simultaneously by a pump 31 into a pipe coil 33 which is heated to vaporize at least part of the liquid and form a rapidly flowing turbulent stream.
- dispersion is assured by splitting the efuent from coil 33 and passing the resulting two streams into a pair of diametrically opposed injector nozzles 35 and 37 which discharge high velocity jets against one another with great forcewithin a chamber 39.
- the particles against one another they are further disintegrated tothe extremely line size desired inthe ultimate products.
- the downstream side of the chamber 39 constitutes a cooler 41 wherein the product is suddenly cooled by direct or indirect heat exchange with a fluid, after which the resulting dispersion is discharged either for storage or for direct consumption in a chemical process.
- Example I Using the apparatus shown in Fig. 1, a large pool of molten sodium is maintained at a temperature of 2509 F. in the tank 11, and a pool of deobase kerosene at a temperature of F. in the tank 19. To assist dispersion the kerosene contains.0.5% of linseedfoil as a dispersing agent.
- the sodium and kerosene are pumped at rates of 200 pounds per hour each into conjunction with one another at the entranceY of heater coil 17 composedi of 1A inch iron pipe 200feet long, the pressure being 200 pounds per square inch gauge-(p. s. i. g.).
- sodium particles will have a ⁇ particle size distribution
- Microns Percent of particles Less than 1 41
- Example II A dispersion ofsulfur in a water solution containing 12% ammonium caseinate is prepared by melting sulfur in tank ⁇ 11 and passing the molten sulfur together with hot water solution from tank 19 in equal quantities at arate of 300 pounds per hour each and a pressure of 250 p. s. i..g. into a pipe coil 17 as described above. The contents of the coil are heated ⁇ to a maximum temperature of 410 F. so that about halfV of the water solution-is vaporized and the liquid sulfur is converted by the turbulence andv high velocity. into tiny droplets which continually reenter the water phase and are dispersed therein. Upon entering cooler 23 at atmospheric pressure there is formed a stable suspension of sulfur particles in water solution.
- Example III Using the apparatus shown in Fig. 2 a slurry is made up in tank 29 of 50% solid parain wax particles in a water solution containing 12% of sodium caseinate as a dispersing agent. pounds per hour and a pressure of 200 p. s. i. g. intoa 1A; inch heater coil 33 250 feet long wherein the slurry is heated to 400 F., the wax melting and being converted by moderate turbulence and velocity into droplets owing alongv with steam and water in the coil.
- the apparatus shown in Fig. 2 a slurry is made up in tank 29 of 50% solid parain wax particles in a water solution containing 12% of sodium caseinate as a dispersing agent. pounds per hour and a pressure of 200 p. s. i. g. intoa 1A; inch heater coil 33 250 feet long wherein the slurry is heated to 400 F., the wax melting and being converted by moderate turbulence and velocity into droplets owing alongv with steam and water in the coil.
- a method for producing a dispersion of a rst normally solid substance in a liquid dispersion medium which z is a non solvent therefor comprising simultaneously passf ing said iirst substance and said liquid together in a Vstream through a heating zone; heating said mixture suiciently to melt saidrst substance and to vaporize at least a substantial part of said liquid to vapor, while maintaining said iirst substance in a liquid condition; subjecting said mixture and said vapor to high velocity of at least l25 feet per second and turbulent tlow sutcient to break up said first substance to liquid particles of extremely line size; and cooling said mixture and vapor, resolidify the particles of saidlirst substance, to condense said vapor and form a dispersion'ot extremely fine particles of said first substance in said liquid dispersing medium.
- a Amethod in accordance with claim l wherein said mixture is heated sutiiciently to vaporize only part of said mixture, and wherein at least part of said particles ofextremely fine size reenter the unvaporized part of said mixture and are distributed therein prior to said cooling step.
- cooling step 4 is performed by introducing additional disfr v persing medium into said mixture and vapor.
- a method in accordance with claim l wherein said mixture and vapor are at least partly subjected to high 'velocity and turbulent llow by discharging ,atleast two jets thereof against one another at high velocity.
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- Chemical Kinetics & Catalysis (AREA)
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Description
-July 22, 1958 l.. T. WORK 2,844,541
PRODUCTION OF DISPERSIONS 4 f Filed sept. 9, 1955 ice n l 2,844,541 PRODUCTION Vl? D lSPERSIONS Lincoln Thomas Work, Maplewood, N. J., assignor to Texaco Development Corporation, NewYork, N. Y., n
va corporation of Delaware v vApplication September 9, 19,55, Serial No. 533,328
13 claims. (cl. 252-314) v The present linvention relates to la novel method for producing dispersions of variousdi-spersoids in dispers-ing ple.dispersions can be formed ofsodium, sulfur, paran wax and asphalt in various liquid dispersion media such as hydrocarbons, water and the like.
l Manylmeth'odsf of producing colloidal materials have previously been used, such as, for example, the production of colloidal metals by means of'an electric discharge,
the precipitation of colloidal material by'drowning a solu-y tion-in ay non-solvent, the Yprecipitation of linely divided substancesby' chemical action and the reduction of particle sizebyrnechanicalgrinding either in the presence or absence of other solid or liquid material.
The product-ion of emulsions of oils or low melting media. TheV method is applicable-to the production of l n emulsions offone liquid in another, and of suspensions Vof a solid material in a liquid or semi liquid. For examwaxes in j water may be accomplished by mechanical v c means,..such as, for example, shaking or agitating a mechanicalst-irrer, but-in general, the method has been .limited to those..materials.which are liquid, or which can easily be brought into a liquid condition. Furthermore, the various mechanical means for the production of emulsions and suspensions are'generally attended by certain disadvantages, such as, for example, operation on a batch yscale rather than continuously and the necessity forfthe usjejof power for operating the mechanical agitatv ing means, which adds to the cost of operation. In many cases, moreover, rapid agitation 'by mechanical methods 1 gives rise to'excessi-ve foaming.
My improved method for producing a dispersionof'a lfirst `substance in a'liquid dispersion medium comprises simultaneously passing the first substance and the liquid together in astream through a heating zone, which may comprise along'tubular pipe arranged within a furnace.lv
The mixture is heated sufficiently to vap-orize part or all of the liquid dispersion medium to form vapor while maintaining the lirst substance unvaporized. The temperature shouldbesutlicientto melt the rst substance if it isv asolidV or semi'solid.v Then themixture and vapor are subjected to highvelocity and turbulent flow to break.
substance to liquid particles of extremely ne up I,the iirst size.- v v Dispersion of the fine liquid particles in the dispersion medium isexpedited by employing onlyy partial vaporization'of -the dispersion medium, because the fine liquid particles produced during the operation constantly enter into the unvaporized dispersion medium and are dispersed therein. l
When the rst substance is one which reacts readily with some atmospheres it is essential to exclude them during vthe operation. For example both air and water l vapor must `bevexcluded fromcontact with sodium.
The eilluent of mixture and vapor is then cooled to condense .the vapor and solidify yany melted particles, thereby forming a dispersion of extremely ne particles of the tirst substance in the liquid dispersion medium. Ooolingmay be accomplished-by circulating a cooling 2 iluid in indirect heat exchange relationshipwith the efuent, or by injecting cool liquid, such as ladditional dispers-ion medium, directly into the effluent for dilution and cooling thereof.
The method described is operable over a wide range of 4 proportions of dispersion medium and dispersoid. For example, the amount of dispersoid can range from as little as 5% of the mixture by weight to as ymuch as 65%. The heat-ing zone may be within a pipe having dimensions based upon the desired capacity of aplant. Di-
ameters may range from '1/2 to 2 inches for example, and lengths may be as little as and as much more or less. K
The invention is generally applicable to the treatmentV and suspensions of various mercury compounds or copper compounds'in oil, sulfur and sodium in oil, sulfur in, p
water, and many other combinations to be used as fungiand chemical reactants.
cides, insecticides, preservatives, delustrants, pigments,
The dispersion maybe etiected in the presenceof aj v protective material. In general, by the expression`proj tective material is meant'any dispersingagent, wetting f agentor protective colloid. As specic examples of such compositions may be mentioned glyptalmresins, 4,gum
tragacanth, alkali metal salts of the higher fattyacids, .i galliacids and their derivatives, agar-agar, glue,`methyl ,y
cellulose, *sulte cellulose lyes, sodiuml cellulose phthalate, calcium saccharate, sodium cellulose glycollate, gela-Y tin, derivatives of cholesterine, phosphatides, gelloses, v natural and artificial waxes, such as wool waxes, alkylol amine salts, quaternary ammonium compounds, clay, sulfonated tallow, sulfonated oils, alkyl sulfuric esters, kand alkali metal caseinates.
The materials -to 'be dispersed and the dispersing me-A dium may be introduced into the heating zone in any suitable manner, and the proportions of the different com- In carrying out the ponents may be varied as desired. process of the invention, the materials to be dispersed and the dispersing medium are brought together in the desired proportion either by roughly mixing `the material-s in a single container, or by llowing the materialslfrom separate containersv into amixing tube or chamber.
The dispersionsystemrproduced may vary Widely in character*dependinglargely lupon `the materials employed.
Thus,r they may consist of one or more different kinds-*of` .i
solid particles in a liquid suspending medium, bothsolid particles and liquid parti-cles in'a liquid dispersionrnedium,`oronfe or more different kinds of liquid particlesin a liquid dispersion medium. v The dispersion medium may contain more than one component, as for example,.solutions of glycerine and Water (preferably 15.-'20.% water) are very desirable dispersion media for sulfur.
'I'he invention will be described further in detail below with reference to the drawings, wherein:A f
Figs. l and 2 are schematic `flow diagrams showingl two alternative arrangements of apparatus for carrying out the invention.
Referring toFig. 1, the invention will be Vexemplified l as applied to the production of a dispersion of solid particles of sodium-metal 'in a flowable dispersion medium which is inert to sodium and has'a boiling pointabove 2,844,541 l Patented July 22, 17958 ,il
as 1000 feet,
themelting point ofsodium, including among others the following:
Petroleum jelly Cetane Sodiumpuried uap'hthaleneV Nujol Tetralin Toluene Dodecene- Dimethoxy decane Deobase kerosene Fuel oil Heptane Mineral oil No. 33 2 White oil Xylene The `principles of course, also apply toall alkali metals including sodium, lithium, potasiurn, cesium, rubidium, and alloys of one with ,the other.
A mass of sodium metal is melted in the tank 11 by circulating a` hot hydrocarbon liquid in indirect heat exchange relationship therewith. Molten sodium is passed by a pump 13 to the interior of a` heater 15 and into a long pipe coil 17. Simultaneously a liquid dispersion medium such as kerosene from a tank 19 ispassed by a pump21 into conjunction with the stream of molten sodium at the entrance to the coil 17. The kerosene should be above the melting point of sodium, 208.1 F., to prevent solidiication. This can be assured by passing the kerosene through a pipe located within the heater 15 before it meets the sodium.
Thetwo streams of liquid mix intimately together and flow through the coil 17 while the latter is heated in any suitableway. Preferably heating is accomplished by heat exchange with a hot liquid such as a high boiling eutectic mixture of diphenyl and diphenyl oxide sold under the trademark Dowtherm by the Dow Chemical Company (boiling point 258 C.), but heating also may be done by a gas or oil flame. The mixture is heated to a temperature high enough to vaporize all or a substantial portion of the kerosene while maintaining the sodium in a molten state.- Consequently, the velocity and turbulence inthe coil increase considerably as liquid vaporizes, the velocity being at least 25 feet per second, preferably above 100 feet per second, and often several thousand feet per second.
As a result of the high velocity and the agitation produced by the extremely turbulent ow developed in the pipe coil the liquid sodium is converted to tiny molten droplets which impinge against one another and against. the Walls of the tube until they are reduced to an extremely ne particle size such as 10 microns or less and predominantly less than microns, a substantial proportion even being ner than one micron.
The mixture of liquid and vapor then leaves the pipe coil 17 and enters a cooler 23 wherein the Vapor is `condensed, the sodium particles are solidified, and a dispersion is formed of extremely ne solid particles of sodium suspended in kerosene. Cooling may be accomplished by ash cooling as the result of the reduced pressure, by circulating cool hydrocarbon liquid indirectly, or by injecting it directly into the effluent Ifrom the pipe coil 17. If desired, chamber 23 can be a classifier such as a cyclone sep arator to collect the liquid phase while removing vapors therefrom.
The resulting product can be used for performing various chemical reactions in a well known way, asfor rening hydrocarbons, preparing alcohol-free alkoxides, or for halide condensation reactions.
Referring to Fig. 2, there is shown a modied system wherein the substance to be dispersed and the dispersing medium are mixed together in a mixer 29 and then passed simultaneously by a pump 31 into a pipe coil 33 which is heated to vaporize at least part of the liquid and form a rapidly flowing turbulent stream. In this modification dispersion is assured by splitting the efuent from coil 33 and passing the resulting two streams into a pair of diametrically opposed injector nozzles 35 and 37 which discharge high velocity jets against one another with great forcewithin a chamber 39. As a result of impingement of the particles against one another they are further disintegrated tothe extremely line size desired inthe ultimate products.
The downstream side of the chamber 39 constitutes a cooler 41 wherein the product is suddenly cooled by direct or indirect heat exchange with a fluid, after which the resulting dispersion is discharged either for storage or for direct consumption in a chemical process.
Example I Using the apparatus shown in Fig. 1, a large pool of molten sodium is maintained at a temperature of 2509 F. in the tank 11, and a pool of deobase kerosene at a temperature of F. in the tank 19. To assist dispersion the kerosene contains.0.5% of linseedfoil as a dispersing agent.
The sodium and kerosene are pumped at rates of 200 pounds per hour each into conjunction with one another at the entranceY of heater coil 17 composedi of 1A inch iron pipe 200feet long, the pressure being 200 pounds per square inch gauge-(p. s. i. g.).
Before meeting the sodium stream, the kerosene stream;
sodium particles will have a` particle size distribution,
about as follows:
Microns: Percent of particles Less than 1 41 Example II A dispersion ofsulfur in a water solution containing 12% ammonium caseinate is prepared by melting sulfur in tank` 11 and passing the molten sulfur together with hot water solution from tank 19 in equal quantities at arate of 300 pounds per hour each and a pressure of 250 p. s. i..g. into a pipe coil 17 as described above. The contents of the coil are heated `to a maximum temperature of 410 F. so that about halfV of the water solution-is vaporized and the liquid sulfur is converted by the turbulence andv high velocity. into tiny droplets which continually reenter the water phase and are dispersed therein. Upon entering cooler 23 at atmospheric pressure there is formed a stable suspension of sulfur particles in water solution.
Example III Using the apparatus shown in Fig. 2 a slurry is made up in tank 29 of 50% solid parain wax particles in a water solution containing 12% of sodium caseinate as a dispersing agent. pounds per hour and a pressure of 200 p. s. i. g. intoa 1A; inch heater coil 33 250 feet long wherein the slurry is heated to 400 F., the wax melting and being converted by moderate turbulence and velocity into droplets owing alongv with steam and water in the coil. The
eliluent from coil 33 enters the two nozzles 35 and 37 havingl; inch orices, and two jets are discharged against one another at an angle of 180 to cause further disintegration of the `parain droplets to a size small enough tov form a colloidal dispersion in water. Upon passing throughV cooler 41 the mixture is cooled by indirect heat exchange withwater and a dispersion is formed of tiny solid parain. particles in the water solutionof sodium casemate.
Obviously, manymodifcations and Variations of the This slurry is passed at a rate of 400 i invention, as hereinbefore set forth, may be made without departing from the spirit andscope thereof, and therefore only such limitations shc'uld be imposed as are indicated inthe appended claims.
I claim: v 1. A method for producing a dispersion of a rst normally solid substance in a liquid dispersion medium which z is a non solvent therefor comprising simultaneously passf ing said iirst substance and said liquid together in a Vstream through a heating zone; heating said mixture suiciently to melt saidrst substance and to vaporize at least a substantial part of said liquid to vapor, while maintaining said iirst substance in a liquid condition; subjecting said mixture and said vapor to high velocity of at least l25 feet per second and turbulent tlow sutcient to break up said first substance to liquid particles of extremely line size; and cooling said mixture and vapor, resolidify the particles of saidlirst substance, to condense said vapor and form a dispersion'ot extremely fine particles of said first substance in said liquid dispersing medium.
2. A Amethod in accordance with claim l wherein said mixture is heated sutiiciently to vaporize only part of said mixture, and wherein at least part of said particles ofextremely fine size reenter the unvaporized part of said mixture and are distributed therein prior to said cooling step.
3. A method in accordance with claim l wherein said first substance is alkali vmetal and said liquid dispersing `non-solvent for sulfur.
6. A method in accordance with claim l wherein s'aiti` cooling step' is performed :by circulating a cooling lluid in 1 y indirect heat exchange relationship with said mixture and vapor.
7. A method in accordance with claim l wherein said cooling step 4is performed by introducing additional disfr v persing medium into said mixture and vapor.
8. A method in accordance with claim 1 whereinsaidY heating zone is an elongated heated tubular zone, and wherein said mixture and said vapor are subjected to high l velocity and turbulent ow during passage thereof through said tubular zone.
9. A method in accordance with claim l wherein said mixture and vapor are at least partly subjected to high 'velocity and turbulent llow by discharging ,atleast two jets thereof against one another at high velocity.
`l0. A method in accordance with claim 1 wherein said mixture is lirst formed upstream of said heating zone and is then passed into said heating zone. i
ll. A method in accordance with claim l wherein said mixture is formed by p-assing separate streams of said substance and said dispersing medium into said heatingv zone.
l2. A method in accordance with claim ll, also com-Av prising melting said substance, and passing said substance as a molten stream into association with said dispersing medium.
13. A method in accordance with claim wherein said mixture is heated suticiently to vaporize substantially all of said liquid to vapor.
References Cited in the file of this patent UNITED STATES PATENTS 2,021,143
Calcott et al. Nov. 19, 1935 UNITED STATES PATENT OFFICE CERTIFICATE 0F CGRRECTION PatentJ No. 2,844,541 p July 22 1958 Lincoln Thomas Work It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 5, lines 18 and 19, strike out "to condense said Vapor" and insert the same after "vapor" and before the comma in line 1'7, same l column,
.Attesting Oiflcer Commissioner of Patents Signed and sealed this 2nd day of December 1958,
SEAL ttest:
KARL H., .AXLINE ROBERT C. WATSON .Attesting Ocer UNITED STATES PATENT OFFICE CERTIFICATE 0F CORECTION Patent No., 2,844,541 July 22g 1958 Lincoln lihomas Work It is hereby certified that error appears in the printed specification of the' above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 5 lines l8 and 19 y strike out "to condense said vapor" and insert the same after nvapor" and before the somma in line l'7, seme Column Signed and sealed this 2nd day of December 1958c SEAL ttest:
KARL .AXLINE ROBERT C. WATSON Commissioner of Patents
Claims (1)
1. A METHOD FOR PRODUCING A DISPERSION OF A FIRST NORMALLY SOLID SUBSTANCE IN A LIQUID DISPERSION MEDIUM WHICH IS A NON SOLVENT THEREFOR COMPRISING SIMULTANEOUSLY PASSING SAID FIRST SUBSTANCE AND SAID LIQUID TOGETHER IN A STREAM THROUGH A HEATING ZONE; HEATING SAID MIXTURE SUFFICIENTLY TO MELT SAID FIRST SUBSTANCE AND TO VAPORIZE AT LEAST A SUBSTANTIAL PART OF SAID LIQUID TO VAPOR, WHILE MAINTAINING SAID FIRST SUBSTANCE IN A LIQUID CONDITION; SUBJECTING SAID MIXTURE AND SAID VAPOR TO HIGH VELOCITY OF AT LEAST 25 FEET PER SECOND AND TURBULENT FLOW SUFFICIENT TO BREAK UP SAID FIRST SUBSTANCE TO LIQUID PARTICLES OF EXTREMELY FINE SIZE; AND COOLING SAID MIXTURE AND VAPOR, RESOLIDIFY THE PARTICLES OF SAID FIRST SUBSTANCE, TO CONDENSE SAID VAPOR AND FORM A DISPERSION OF EXTREMELY FINE PARTICLES OF SAID FIRST SUBSTANCE IN SAID LIQUID DISPERSING MEDIUM.
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2917345A (en) * | 1957-08-26 | 1959-12-15 | Humble Oil & Refining Company | Process of producing sulfur slurry for transportation thereof |
US3361681A (en) * | 1964-06-12 | 1968-01-02 | Goodyear Tire & Rubber | Titanium tetraiodide suspensions |
US3412034A (en) * | 1963-04-22 | 1968-11-19 | Switzer Brothers Inc | Method for producing fine pigment particles in a liquid vehicle |
US4132666A (en) * | 1975-10-09 | 1979-01-02 | Japan Synthetic Rubber Company, Limited | Process for preparing alkali metal dispersions |
US4136043A (en) * | 1973-07-19 | 1979-01-23 | The Lubrizol Corporation | Homogeneous compositions prepared from dimercaptothiadiazoles |
US4302237A (en) * | 1977-06-06 | 1981-11-24 | Union Oil Company Of California | Sulfur product and method |
US4326875A (en) * | 1978-12-26 | 1982-04-27 | Union Oil Company Of California | Sulfur product and method |
US5236624A (en) * | 1987-03-16 | 1993-08-17 | Exxon Chemical Patents Inc. | Dispersions and emulsions |
US7291295B2 (en) * | 2000-08-25 | 2007-11-06 | Sociedad Espanola De Carburos Metalicos, S.A. | Method for precipitating finely divided solid particles |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2021143A (en) * | 1932-09-30 | 1935-11-19 | Du Pont | Production of dispersions |
-
1955
- 1955-09-09 US US533328A patent/US2844541A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2021143A (en) * | 1932-09-30 | 1935-11-19 | Du Pont | Production of dispersions |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2917345A (en) * | 1957-08-26 | 1959-12-15 | Humble Oil & Refining Company | Process of producing sulfur slurry for transportation thereof |
US3412034A (en) * | 1963-04-22 | 1968-11-19 | Switzer Brothers Inc | Method for producing fine pigment particles in a liquid vehicle |
US3361681A (en) * | 1964-06-12 | 1968-01-02 | Goodyear Tire & Rubber | Titanium tetraiodide suspensions |
US4136043A (en) * | 1973-07-19 | 1979-01-23 | The Lubrizol Corporation | Homogeneous compositions prepared from dimercaptothiadiazoles |
US4132666A (en) * | 1975-10-09 | 1979-01-02 | Japan Synthetic Rubber Company, Limited | Process for preparing alkali metal dispersions |
US4302237A (en) * | 1977-06-06 | 1981-11-24 | Union Oil Company Of California | Sulfur product and method |
US4326875A (en) * | 1978-12-26 | 1982-04-27 | Union Oil Company Of California | Sulfur product and method |
US5236624A (en) * | 1987-03-16 | 1993-08-17 | Exxon Chemical Patents Inc. | Dispersions and emulsions |
US7291295B2 (en) * | 2000-08-25 | 2007-11-06 | Sociedad Espanola De Carburos Metalicos, S.A. | Method for precipitating finely divided solid particles |
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